09/05/2024 | Fulltime | York | CV-LibraryCK Group are recruiting for a Scientist II – Clinical Chemistry to join a leading laboratory, specialising in clinical trials, central lab services and toxicology. Candidates for this role must have a minimum of 12 months experience in Clinical Chemistry from a diagnostic or clinical trials
Save for laterRegister your CV09/05/2024 | Fulltime | Wolverhampton | CV-Library | £35,000 - £45,000 / Year Litigator A Civil Litigator is required by a law firm based near Stafford, acting for a wide variety of both claimant and defendant work representing individuals and businesses in relation to matters including contractual disputes, counter fraud, construction claims, clinical negligence claims
Save for laterRegister your CV09/05/2024 | Fulltime | Maidenhead | CV-Library | £22 - £35 / Hour For Clinical Trials. They are the primary interface between global functions and affiliates to deliver clinical development regulatory strategies, operations and outcomes. Key Responsibilities § Manage a portfolio of CTAs including preparation and distribution of documentation associated with new initial CTAs
Save for laterRegister your CV09/05/2024 | Fulltime | Lincoln | CV-Library | £25,000 - £35,000 / Year A busy caseload of clinical negligence cases, ranging from taking new instructions through to trial or settlement of litigated cases. The successful candidate will also assist senior solicitors with high-value complex claims. They are happy to take applications from Paralegals; NQ Solicitors or NQ Legal
Save for laterRegister your CV09/05/2024 | Fulltime | Hillingdon | CV-Library | - £45 / Hour With appropriate contingency strategies. Review the preparation of M2 and 3 CMC components of filings and assess fitness of purpose for submission in the relevant countries. Manage strategy and execution for all regulatory CMC submissions (e.g. late stage clinical trials, variations, extensions and marketing
Save for laterRegister your CV08/05/2024 | Fulltime | Marlow | CV-LibraryAre finalised according to strict deadlines and within budget. The role will also focus on ensuring clinical trial comparator supplies and ancillaries are delivered to clients on time with all relevant documents. As our Team Administrator - Coordinator you will be responsible for - Assisting Business Managers
Save for laterRegister your CV08/05/2024 | Fulltime | Tring | CV-LibraryLevel, proactively ensuring our clients’ Trial Master Files (TMFs) are achieving an inspection ready state. They are an integral part of the study team, becoming a single point of contact to help maintain TMF health, consistency, and compliance across clinical trials within the organisation. What are we
Save for laterRegister your CV08/05/2024 | Fulltime | Bollington | CV-LibraryDiscipline. This may include science/ research focused subjects, epidemiology, public health, medicine or health economics. - Basic PowerPoint, Excel, and Word skills. - Research experience, (academic research, non-interventional studies, clinical trials, market research etc) - A high level of interpersonal
Save for laterRegister your CV08/05/2024 | Fulltime | Tring | CV-LibraryHealth, consistency, and compliance across clinical trials within the organisation. What are we offering our Trial Master File Study Owner? The salary will be commensurate with the candidate’s experience 25 days holiday plus BH (increasing to 27 after qualifying service) 8% employer pension contribution
Save for laterRegister your CV07/05/2024 | Fulltime | Kettering | CV-LibrarySpecialising in the scientific, engineering, clinical, pharmaceutical, food/FMCG, energy & renewables, biotech, chemical and medical device sectors. As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed
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